4.7 Article

Nanogold-Carried Graphene Oxide: Anti-Inflammation and Increased Differentiation Capacity of Mesenchymal Stem Cells

期刊

NANOMATERIALS
卷 11, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/nano11082046

关键词

gold nanoparticles; graphene oxide; mesenchymal stem cells; anti-inflammation; differentiation

资金

  1. China Medical University Hospital [DMR-105-057]
  2. Ministry of Science and Technology [MOST 109-2314-B-075B-011-MY3]

向作者/读者索取更多资源

Graphene-based nanocomposites, particularly gold nanoparticle-decorated GO (GO-Au), exhibit excellent physicochemical properties and have potential applications in tissue engineering. In this study, GO-Au (x2) showed significantly increased cell viability of MSCs, good anti-oxidative ability, immune response modulation, and platelet activity inhibition. Moreover, the Au-deposited GO nanocomposites demonstrated superior efficacy in enhancing cell motility, promoting various MSCs-derived cell types of differentiation, and reducing fibrotic formation and M1 macrophage polarization in an implanted animal model. These results suggest that Au-deposited GO nanocomposites have great potential as nanocarriers for tissue engineering and effective strategies for anti-inflammation.
Graphene-based nanocomposites such as graphene oxide (GO) and nanoparticle-decorated graphene with demonstrated excellent physicochemical properties have worthwhile applications in biomedicine and bioengineering such as tissue engineering. In this study, we fabricated gold nanoparticle-decorated GO (GO-Au) nanocomposites and characterized their physicochemical properties using UV-Vis absorption spectra, FTIR spectra, contact angle analyses, and free radical scavenging potential. Moreover, we investigated the potent applications of GO-Au nanocomposites on directing mesenchymal stem cells (MSCs) for tissue regeneration. We compared the efficacy of as-prepared GO-derived nanocomposites including GO, GO-Au, and GO-Au (x2) on the biocompatibility of MSCs, immune cell identification, anti-inflammatory effects, differentiation capacity, as well as animal immune compatibility. Our results showed that Au-deposited GO nanocomposites, especially GO-Au (x2), significantly exhibited increased cell viability of MSCs, had good anti-oxidative ability, sponged the immune response toward monocyte-macrophage transition, as well as inhibited the activity of platelets. Moreover, we also validated the superior efficacy of Au-deposited GO nanocomposites on the enhancement of cell motility and various MSCs-derived cell types of differentiation including neuron cells, adipocytes, osteocytes, and endothelial cells. Additionally, the lower induction of fibrotic formation, reduced M1 macrophage polarization, and higher induction of M2 macrophage, as well as promotion of the endothelialization, were also found in the Au-deposited GO nanocomposites implanted animal model. These results suggest that the Au-deposited GO nanocomposites have excellent immune compatibility and anti-inflammatory effects in vivo and in vitro. Altogether, our findings indicate that Au-decorated GO nanocomposites, especially GO-Au (x2), can be a potent nanocarrier for tissue engineering and an effective clinical strategy for anti-inflammation.

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